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The Effect of Topical Tranexamic Acid in Endoscopic Sinus Surgery: A Triple Blind Randomized Clinical Trial.
Achour, Imen; Ben Rhaiem, Zied; Thabet, Wadii; Jdidi, Jihene; Mnejja, Malek; Hammami, Bouthaina; Chakroun, Amine; Charfeddine, Ilhem.
Afiliação
  • Achour I; Department of Otorhinolaryngology, Habib Bourguiba Hospital, Sfax, Tunisia.
  • Ben Rhaiem Z; University of Sfax, Sfax, Tunisia.
  • Thabet W; Department of Otorhinolaryngology, Valenciennes Hospital, Valenciennes, France.
  • Jdidi J; Department of Otorhinolaryngology, Habib Bourguiba Hospital, Sfax, Tunisia.
  • Mnejja M; University of Sfax, Sfax, Tunisia.
  • Hammami B; University of Sfax, Sfax, Tunisia.
  • Chakroun A; Department of Epidemiology and Preventive Medicine, Hedi Chaker Hospital, Sfax, Tunisia.
  • Charfeddine I; Department of Otorhinolaryngology, Habib Bourguiba Hospital, Sfax, Tunisia.
Ann Otol Rhinol Laryngol ; 132(3): 244-249, 2023 Mar.
Article em En | MEDLINE | ID: mdl-35373603
ABSTRACT

OBJECTIVE:

Our aim is to evaluate the effect of topical tranexamic acid (TA) on bleeding and surgical quality field in the functional endoscopic sinus surgery (FESS).

METHODS:

A total of 74 patients who underwent FESS due to chronic rhinosinusitis were included. The patients were randomized into 2 groups. TA group (n = 37) received a topical cotton pledget soaked with TA and placebo (PL) group (n = 37) received a pledget soaked with saline solution.

RESULTS:

A significant effect was noted for the TA group versus the PL group in the grade 1 of the Boezaart scale at 35 minutes (4 for TA group and no case for PL group). This effect was absent for higher grades. We did not notice a significant effect between the 2 groups at 5 minutes. Blood loss was 359 ml in the TA group versus 441 ml in the PL group. No significant change was observed between the 2 groups concerning the blood parameters. No side effects were reported.

CONCLUSION:

Despite its safety when administrated locally and its low cost, TA provides limited effect on quality of surgical field after 35 minutes of the start of FESS in the patients with chronic rhinosinusitis. This effect was absent at the start of the intervention and when analyzing the blood loss and hematologic parameters.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinusite / Ácido Tranexâmico / Antifibrinolíticos Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Ann Otol Rhinol Laryngol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Tunísia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinusite / Ácido Tranexâmico / Antifibrinolíticos Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Ann Otol Rhinol Laryngol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Tunísia